Department of Internal Medicine, Michigan State University, East Lansing, MI, USA.
Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, TX, USA.
Cardiovasc Revasc Med. 2022 Mar;36:18-24. doi: 10.1016/j.carrev.2021.04.019. Epub 2021 Apr 22.
Left atrial appendage closure (LAAC) devices are an alternative therapy in non-valvular atrial fibrillation (NVAF) patients with contraindications to oral anticoagulation (OAC). However, there are limited data about the clinical outcomes of LAAC devices compared to medical treatment.
A comprehensive research for studies comparing LAAC devices and OAC for patients with NVAF was performed from inception to January 1, 2021. A meta-analysis was performed using a random effect model to calculate odds ratios (OR) with 95% confidence intervals (CIs).
Five studies were eligible that included a total of 4778 patients with a median-weighted follow-up period was 2.6 years. Compared to OAC, the LAAC device arm was associated with a lower risk of the composite of stroke, systemic embolism, and cardiovascular death (OR 0.71; 95% CI 0.51-1.00; p = 0.05). LAAC device arm was also associated with a lower risk of all-cause mortality (OR of 0.60, 95% CI 0.46-0.77; p < 0.0001), cardiovascular mortality (OR of 0.57, 95% CI 0.46-0.70; p < 0.00001), hemorrhagic stroke (OR of 0.19, 95% CI 0.07-0.50; p= 0.0006), all major bleeding (OR of 0.61, 95% CI 0.43-0.88; p = 0.007) and non-procedural major bleeding (OR of 0.46, 95% CI 0.32-0.65; p < 0.0001). There was no significant difference in all stroke, ischemic stroke, and systemic embolization between the two groups.
Our meta-analysis showed lower all-cause mortality, cardiovascular mortality, hemorrhagic stroke, major bleeding, non-procedural major bleeding and the composite of stroke, systemic embolism, and cardiovascular death in the LAAC device arm when compared to OAC. However, the risk of all stroke, ischemic stroke, and systemic embolism were similar between the two arms.
左心耳封堵 (LAAC) 装置是伴有抗凝禁忌的非瓣膜性心房颤动 (NVAF) 患者的替代治疗方法。然而,与药物治疗相比,关于 LAAC 装置的临床结果的数据有限。
从研究开始到 2021 年 1 月 1 日,对比较 LAAC 装置和 NVAF 患者 OAC 的研究进行了全面检索。使用随机效应模型进行荟萃分析,计算优势比 (OR) 和 95%置信区间 (CI)。
符合条件的五项研究共纳入 4778 例患者,中位随访时间为 2.6 年。与 OAC 相比,LAAC 装置组发生卒中、全身性栓塞和心血管死亡的复合终点风险较低 (OR 0.71;95%CI 0.51-1.00;p=0.05)。LAAC 装置组的全因死亡率 (OR 0.60,95%CI 0.46-0.77;p<0.0001)、心血管死亡率 (OR 0.57,95%CI 0.46-0.70;p<0.00001)、出血性卒中 (OR 0.19,95%CI 0.07-0.50;p=0.0006)、所有主要出血 (OR 0.61,95%CI 0.43-0.88;p=0.007) 和非程序主要出血 (OR 0.46,95%CI 0.32-0.65;p<0.0001) 的风险也较低。两组之间的所有卒中、缺血性卒中和全身性栓塞无显著差异。
我们的荟萃分析表明,与 OAC 相比,LAAC 装置组的全因死亡率、心血管死亡率、出血性卒中、主要出血、非程序主要出血和卒中、全身性栓塞和心血管死亡的复合终点发生率较低。然而,两组之间的所有卒中、缺血性卒中和全身性栓塞的风险相似。